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Hereditary Cancer in Clinical Practice cover

Hereditary Cancer in Clinical Practice

IF2.4
Papers24
Citations593
Journal Papers 24
Publication Date
Importance of genetic testing in childhood cancer survivors for hereditary cancer predisposition syndromes
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deleteUrbas, Anja; Usaj, Polona; Seruga, Bostjan; Krajc, Mateja; Hotujec, Simona; Stegel, Vida; Zaletel, Lorna Zadravec
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Impact of germline MMR gene variants on immune checkpoint inhibitors response in patients with MSI-H/dMMR digestive cancers: a retrospective cohort analysis
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deleteDardenne, Antoine; Loisel, Camille; Pellat, Anna; Perrier, Alexandre; Metras, Julie; Samaille, Thomas; Parc, Yann; Leclerc, Julie; Cohen, Romain; Andre, Thierry
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Breast cancer specialists' experiences and attitudes towards mainstream genetic testing for patients with breast cancer
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deleteAllan, Kirsten; Cicciarelli, Linda; Beard, Catherine; Lindeman, Geoffrey J.; Mann, G. Bruce; James, Paul A.; Forrest, Laura E.
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Monitoring and treatment patterns of von Hippel-Lindau disease-associated central nervous system hemangioblastomas
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deleteJonasch, Eric; Song, Yan; Freimark, Jonathan; Mohan, Manasi; Signorovitch, James; Sundaram, Murali
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Challenging interpretation of low-level PTCH1 mosaicism in patients with clinically diagnosed Gorlin syndrome: a case series and review of the literature
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deleteDwarte, Tanya M.; Alli, Rozanna; Srinivasa, Shweta; Noon, Fallon; Kimmantudawage, Sumudu Perera; Gordon, Lisa; Beshay, Victoria; Joshua, Anthony M.; Araujo, Raquel Ruiz; Jalilian, Chris; Thomas, David M.; Smith, Miriam J.; Winship, Ingrid; Ballinger, Mandy L.; Li, Minmin; Tucker, Katherine M.; Courtney, Eliza K.
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Case report: a rare BRCA1 de novo variant in a female with breast cancer
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deleteDencker, Carlotta; Strehlow, Vincent; Aktas, Bahriye; Lemke, Johannes; Hentschel, Julia
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A retrospective analysis of risk-reducing salpingo-oophorectomy performed in women diagnosed with hereditary breast and ovarian cancer at our institution
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deleteShimizu, Yusaku; Kitai, Miho; Akada, Masashi; Maeda, Michihide; Yamabe, Eri; Kakubari, Reisa; Hisa, Tsuyoshi; Kamiura, Shoji
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Utilization of care and alignment of screening with NCCN guidelines for patients with Lynch syndrome: a retrospective cohort study
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deleteLowry, Christina; Laurent, Cecile; Bindra, Ameek K.; Powell, C. Bethan; Garcia, Christine
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Genomic profiling in Bulgarian women with ovarian cancer: a dual-sample NGS approach
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deleteKamburova, Zornitsa; Popovska, Savelina; Tsvetkov, Chavdar
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Two novel multiple endocrine neoplasia type 1 variants caused thymic neuroendocrine tumor: a case report
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deleteDai, Zi; Zhang, Jing; Wang, Jing; Ma, Leshi; Liao, Pei; Deng, Xiaojie; Li, Zhenxiang; Luo, Zhijie; Guan, Jieshan
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Primary and metastatic brain tumours in hereditary cancer syndromes: case reports with and literature review
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deleteRobaczynska, Joanna; Kiljanczyk, Milena; Stachowski, Adam; Lubinski, Krzysztof; Dodopoulos, Angelos; Benali, Rayane; Kiljanczyk, Adam; Becht, Rafal; Cybulski, Cezary; Gronwald, Jacek; Lubinski, Jan
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Decisional conflict in women with a BRCA1 or BRCA2 pathogenic variant who have not elected for risk-reducing salpingo-oophorectomy
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deleteMetcalfe, Kelly A.; Kinney, Anita Y.; Narod, Steven A.; Poll, Aletta; Armel, Susan; Lombardi, Lucia; Tavangar, Farideh; Pal, Tuya
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Skin cancer risk in hereditary mixed cancer syndromes
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deleteNikkola, Veera; Alakoski, Anna; Mecklin, Jukka-Pekka; Seppala, Toni T.; Nikkola, Jussi; Schrader, Kashmintan
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Clinical characteristics and healthcare burden of neurofibromatosis type 1 in Saudi Arabia: a single centre experience
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deleteAlmuqbil, Mohammed A.; Al Ammari, Maha; Al Dhayyan, Nada S.; Kaithathara, Seena Thomas; Al Balwi, Mohamed
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Contribution of MLH1, MSH2, and MSH6 large genomic rearrangements to Pakistani colorectal cancer patients
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deleteNaeemi, Humaira; Muhammad, Noor; Loya, Asif; Yusuf, Muhammed Aasim; Rashid, Muhammad Usman
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The genetic puzzle of FAP: exploring novel diagnostic approaches for APC/MUTYH-negative case
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deleteGrot, Natalia; Kazimierczyk, Marek; Szuman, Marcin; Kaczmarek-Rys, Marta; Kryszczynska, Alicja; Dziechciowska, Iga; Knaur, Monika; Hnatyszyn, Andrzej; Hryhorowicz, Szymon; Plawski, Andrzej
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Molecular markers associated with elevated colorectal cancer risk: a mini review
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deleteSzuman, Marcin; Kazimierczyk, Marek; Grot, Natalia; Kaczmarek-Rys, Marta; Kryszczynska, Alicja; Dziechciowska, Iga; Knaur, Monika; Hnatyszyn, Andrzej; Hryhorowicz, Szymon; Plawski, Andrzej
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Tumour spectrum, distinguishing features and management recommendations for NTHL1-associated tumour syndrome: a systematic review
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deleteGao, Weilun; Liao, Chuyi; Buchanan, Daniel D.; Macrae, Finlay; de Voer, Richarda M.
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